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IRCT20180918041059N1 IRCT 2018-10-02 Esfahan University of Medical Sciences Comparison between Superficial and Deep Dry Needling on Surface Electromyography of Myofascial Trigger Point Comparison between immediate effect of Superficial and Deep Dry Needling on Surface Electromyography in women with Upper Trapezius Active Myofascial Trigger Point 2017-11-21 anticipated 50 Complete https://irct.ir/trial/33981 interventional Randomization: Randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: simple randomization through random - number table, Blinding description: In this study, a double blinded method is used in which both the participants and the evaluator are unaware about the type and group of treatment . N/A upper trapezius myofascial trigger point. Intervention 1: Intervention group: For first group, deep needle (height: 40 millimeter, diameter: 0.2 millimeter) inserted into myofascial trigger point with 10 times in and out movement. Intervention 2: Intervention group: for second group the superficial needle (height: 13 millimeter, diameter: 0.2 millimeter) inserted into superficial tissue above the myofascial trigger point and kept in for 2 to 3 minutes. Undecided - It is not yet known if there will be a plan to make this available Justification or reason for indecision in sharing IPD is No more information
public Navid Taheri
Isfahan University Of Medical Sciences, Hezarjerib Ave, Isfahan, Iran
Isfahan Iran (Islamic Republic of) 87746-73461 +98 31 3792 5043 n_taheri@rehab.mui.ac.ir Esfahan University of Medical Sciences scientific Navid Taheri
Isfahan University Of Medical Sciences, Hezarjerib Ave, Isfahan, Iran
Isfahan Iran (Islamic Republic of) 81746-73461 +98 31 3792 5043 n_taheri@rehab.mui.ac.ir Esfahan University of Medical Sciences Iran (Islamic Republic of) Literate women 18 to 50 years Unilateral neck or shoulder pain with at least one active Myofascial Trigger Point in the upper trapezius muscle for at least 3 months Not receiving analgesic therapy by patients 18 years 50 years Female Fear of dry needling Local and systematic infection People with fibromyalgia and neck osteoarthritis People who used anticoagulant drugs Acute muscle trauma History of neck or shoulder surgery History of receiving dry needling at last 6 months Receiving physical therapy in the past month Dry needling contraindications like pregnancy, allergy, existence of implants and pacemakers M62 Other disorders of muscle Rehabilitation Rehabilitation Intervention group: For first group, deep needle (height: 40 millimeter, diameter: 0.2 millimeter) inserted into myofascial trigger point with 10 times in and out movement. Intervention group: for second group the superficial needle (height: 13 millimeter, diameter: 0.2 millimeter) inserted into superficial tissue above the myofascial trigger point and kept in for 2 to 3 minutes Surface electromyography activity. Timepoint: Before, immediately and one week after the intervention. Method of measurement: Surface electromyography device. Neck disability. Timepoint: Before and one week after the intervention. Method of measurement: Neck disability index questionnaire. Esfahan University of Medical Sciences Approved 2017-07-25 Ethics committee of Isfahan University of Medical Sciences Room 209, 2nd Floor, Building number 4, Isfahan University of Medical Sciences, Hezarjerib Ave Isfahan Isfehan Iran (Islamic Republic of)